A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045477



Internal ID18788008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:59896899..59946670hg38UCSC Ensembl
Innerchr11:59664372..59714143hg19UCSC Ensembl
Innerchr11:59420948..59470719hg18UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3849772
hg1949772
hg1849772
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3710610
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045477
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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